5-Bromoisoquinolin-8-amine is a chemical compound characterized by its isoquinoline structure, which features a fused benzene and pyridine ring system. The presence of a bromine atom at the 5-position and an amino group at the 8-position contributes to its unique reactivity and potential applications in medicinal chemistry. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents, depending on the specific conditions. Its molecular structure allows for various functionalization possibilities, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. The bromine substituent can participate in nucleophilic substitution reactions, while the amino group can engage in hydrogen bonding and serve as a site for further chemical modifications. Additionally, compounds like 5-bromoisoquinolin-8-amine are often studied for their biological activities, including potential anti-cancer and anti-inflammatory properties. Safety and handling precautions should be observed, as with many halogenated amines, due to potential toxicity and environmental impact.

5-bromoisoquinolin-8-amine

90721-35-0: 5-Bromoisoquinolin-8-amine is a chemical compound characterized by its isoquinoline structure, which features a fused benzene and pyridine ring system. The presence of a bromine atom at the 5-position and an amino group at the 8-position contributes to its unique reactivity and potential applications in medicinal chemistry. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents, depending on the specific conditions. Its molecular structure allows for various functionalization possibilities, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. The bromine substituent can participate in nucleophilic substitution reactions, while the amino group can engage in hydrogen bonding and serve as a site for further chemical modifications. Additionally, compounds like 5-bromoisoquinolin-8-amine are often studied for their biological activities, including potential anti-cancer and anti-inflammatory properties. Safety and handling precautions should be observed, as with many halogenated amines, due to potential toxicity and environmental impact.

CAS 90721-35-0

5-bromoisoquinolin-8-amine

5-BROMO-8-ISOQUINOLINEAMINE

Ref: IN-DA00GRUS

8-Amino-5-bromoisoquinoline

Ref: 54-OR40222

5-Bromoisoquinolin-8-ylamine

Ref: 10-F233408